A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6760896



Internal ID10168088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:76692358..76693021hg38UCSC Ensembl
Outerchr11:76403402..76404065hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744793
Supporting Variants
SamplesSSM061
Known GenesGUCY2EP
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6760896
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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